Canonical Allele Identifier: CA14390434
Gene: AATK HGNC NCBI

Linked Data

dbSNP Id: rs7220048

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81144773T>C , CM000679.2:g.81144773T>C GRCh38
NC_000017.10:g.79118573T>C , CM000679.1:g.79118573T>C GRCh37
NC_000017.9:g.76733168T>C NCBI36
NG_029981.1:g.26300A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000326724.9:c.56-10272A>G MANE Select ENSP00000324196.4:n.56-10272A>G
ENST00000326724.8:c.56-10272A>G ENSP00000324196.4:n.56-10272A>G
ENST00000374792.6:c.56-10272A>G ENSP00000363924.2:n.56-10272A>G
ENST00000572798.1:n.274-10272A>G
NM_001080395.2:c.56-10272A>G NP_001073864.2:n.56-10272A>G
XM_005257855.2:c.56-10272A>G XP_005257912.1:n.56-10272A>G
XM_006722193.2:c.-89-10272A>G XP_006722256.1:n.-89-10272A>G
XM_006722194.2:c.56-10272A>G XP_006722257.1:n.56-10272A>G
XM_006722196.1:c.-89-10272A>G XP_006722259.1:n.-89-10272A>G
XR_934622.1:n.131-10272A>G
XM_006722196.2:c.-89-10272A>G XP_006722259.1:n.-89-10272A>G
XM_017025421.1:c.-120-13568A>G XP_016880910.1:n.-120-13568A>G
XR_001752699.1:n.131-10272A>G
XR_002958094.1:n.131-10272A>G
NM_001080395.3:c.56-10272A>G MANE Select NP_001073864.2:n.56-10272A>G